Arbutin (BioDeep_00000000220)

 

Secondary id: BioDeep_00000406115

human metabolite PANOMIX_OTCML-2023 Endogenous natural product


代谢物信息卡片


(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)tetrahydro-2H-pyran-3,4,5-triol

化学式: C12H16O7 (272.0896)
中文名称: 楊梅葉甘, 熊果叶甙, 熊果酚甙, 熊果苷, 熊果素
谱图信息: 最多检出来源 Homo sapiens(otcml) 4.03%

分子结构信息

SMILES: C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O
InChI: InChI=1S/C12H16O7/c13-5-8-9(15)10(16)11(17)12(19-8)18-7-3-1-6(14)2-4-7/h1-4,8-17H,5H2/t8-,9-,10+,11-,12-/m1/s1

描述信息

Hydroquinone O-beta-D-glucopyranoside is a monosaccharide derivative that is hydroquinone attached to a beta-D-glucopyranosyl residue at position 4 via a glycosidic linkage. It has a role as a plant metabolite and an Escherichia coli metabolite. It is a beta-D-glucoside and a monosaccharide derivative. It is functionally related to a hydroquinone.
Extracted from the dried leaves of bearberry plant in the genus Arctostaphylos and other plants commonly in the Ericaceae family, arbutin is a beta-D-glucopyranoside of [DB09526]. It is found in foods, over-the-counter drugs, and herbal dietary supplements. Most commonly, it is an active ingredient in skincare and cosmetic products as a skin-lightening agent for the prevention of melanin formation in various skin conditions that involve cutaneous hyperpigmentation or hyperactive melanocyte function. It has also been used as an anti-infective for the urinary system as well as a diuretic. Arbutin is available in both natural and synthetic forms; it can be synthesized from acetobromglucose and [DB09526]. Arbutin is a competitive inhibitor of tyrosinase (E.C.1.14.18.1) in melanocytes, and the inhibition of melanin synthesis at non-toxic concentrations was observed in vitro. Arbutin was shown to be less cytotoxic to melanocytes in culture compared to [DB09526].
Arbutin is a natural product found in Grevillea robusta, Halocarpus biformis, and other organisms with data available.
See also: Arctostaphylos uva-ursi leaf (part of); Arbutin; octinoxate (component of); Adenosine; arbutin (component of) ... View More ...
Arbutin, also known as hydroquinone-O-beta-D-glucopyranoside or P-hydroxyphenyl beta-D-glucopyranoside, is a member of the class of compounds known as phenolic glycosides. Phenolic glycosides are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. Arbutin is soluble (in water) and a very weakly acidic compound (based on its pKa). Arbutin can be found in a number of food items such as guava, lingonberry, irish moss, and rowal, which makes arbutin a potential biomarker for the consumption of these food products. Arbutin is a glycoside; a glycosylated hydroquinone extracted from the bearberry plant in the genus Arctostaphylos among many other medicinal plants, primarily in the Ericaceae family. Applied topically, it inhibits tyrosinase and thus prevents the formation of melanin. Arbutin is therefore used as a skin-lightening agent. Very tiny amounts of arbutin are found in wheat, pear skins, and some other foods. It is also found in Bergenia crassifolia. Arbutin was also produced by an in vitro culture of Schisandra chinensis .
A monosaccharide derivative that is hydroquinone attached to a beta-D-glucopyranosyl residue at position 4 via a glycosidic linkage.
Arbutin is found in apple. Glucoside in pear leaves (Pyrus communis
C471 - Enzyme Inhibitor
CONFIDENCE standard compound; INTERNAL_ID 1335; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 6126; ORIGINAL_PRECURSOR_SCAN_NO 6123
CONFIDENCE standard compound; INTERNAL_ID 1335; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 6107; ORIGINAL_PRECURSOR_SCAN_NO 6104
CONFIDENCE standard compound; INTERNAL_ID 1335; DATASET 20200303_ENTACT_RP_MIX504; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 811; ORIGINAL_PRECURSOR_SCAN_NO 808
CONFIDENCE standard compound; INTERNAL_ID 1335; DATASET 20200303_ENTACT_RP_MIX504; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 806; ORIGINAL_PRECURSOR_SCAN_NO 804
CONFIDENCE standard compound; INTERNAL_ID 1335; DATASET 20200303_ENTACT_RP_MIX504; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 813; ORIGINAL_PRECURSOR_SCAN_NO 811
CONFIDENCE standard compound; INTERNAL_ID 1335; DATASET 20200303_ENTACT_RP_MIX504; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 832; ORIGINAL_PRECURSOR_SCAN_NO 828
CONFIDENCE standard compound; INTERNAL_ID 1335; DATASET 20200303_ENTACT_RP_MIX504; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 817; ORIGINAL_PRECURSOR_SCAN_NO 816
Arbutin (β-Arbutin) is a competitive inhibitor of tyrosinase, with Kiapp values of 1.42 mM for monophenolase; 0.9 mM for diphenolase. Arbutin is also used as depigmenting agents[1]. Arbutin is a natural polyphenol isolated from the bearberry plant Arctostaphylos uvaursi, possesses with anti-oxidant, anti-inflammatory and anti-tumor properties[2][3].
Arbutin (β-Arbutin) is a competitive inhibitor of tyrosinase, with Kiapp values of 1.42 mM for monophenolase; 0.9 mM for diphenolase. Arbutin is also used as depigmenting agents[1]. Arbutin is a natural polyphenol isolated from the bearberry plant Arctostaphylos uvaursi, possesses with anti-oxidant, anti-inflammatory and anti-tumor properties[2][3].

同义名列表

104 个代谢物同义名

(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)tetrahydro-2H-pyran-3,4,5-triol; (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)tetrahydropyran-3,4,5-triol; (2S,3R,4S,5S,6R)-2-(4-hydroxyphenoxy)-6-methylol-tetrahydropyran-3,4,5-triol; (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(4-oxidanylphenoxy)oxane-3,4,5-triol; (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol; Arbutin, European Pharmacopoeia (EP) Reference Standard; alpha-Arbutin; 4-Hydroquinone-alpha-D-glucopyranoside; Arbutin, primary pharmaceutical reference standard; ICEKING Freckle Removing Whitening Facial Cleanser; 4-Hydroxyphenyl b-D-glucopyranoside, 9CI, 8CI; 5-17-07-00110 (Beilstein Handbook Reference); ISAKNOX WHITE SYMPHONY BRIGHTENING EMULSION; Sooryehan Pure-Whitening Essential Starter; ICEKING Whitening Freckle Removing Essence; ICEKING Freckle Removing Whitening Masque; beta -D-Glucopyranoside, 4-hydroxyphenyl; 4-Hydroxyphenyl-.beta.-D-glucopyranoside; beta-D-Glucopyranoside, 4-hydroxyphenyl-; P-Hydroxyphenyl beta -D-glucopyranoside; beta-D-Glucopyranoside, 4-hydroxyphenyl; I(2)-D-Glucopyranoside, 4-hydroxyphenyl; 4-Hydroxyphenyl-beta-D-glucopyranoside; p-Hydroxyphenyl beta-D-glucopyranoside; 4-Hydroxyphenyl beta-D-glucopyranoside; hydroquinone O-beta-D-glucopyranoside; HYDROQUINONE-.BETA.-D-GLUCOPYRANOSIDE; Hydroquinone-O-beta-D-glucopyranoside; b-D-Glucopyranoside, 4-hydroxyphenyl; 4-Hydroxyphenyl-beta-glucopyranoside; 4E19B706-2013-4401-A1FC-A154DADF42B4; Hydroquinone beta -D-glucopyranoside; p-Hydroxyphenyl β-D-glucopyranoside; Hydroquinone beta-D-glucopyranoside; 4-Hydroxyphenyl β-D-glucopyranoside; p-Hydroxyphenyl b-D-glucopyranoside; Hydroquinone-beta-D-glucopyranoside; Tosowoong Mens Booster Repair Skin; Hydroquinone-O-β-D-glucopyranoside; Hydroquinone-O-b-D-glucopyranoside; Hydroquinone |A-D-glucopyranoside; P-Hydroxyphenyl beta -D-glucoside; 4-Hydroxyphenyl-b-glucopyranoside; 4-Hydroxyphenyl-β-glucopyranoside; Hydroquinone β-D-glucopyranoside; p-Hydroxyphenyl beta-D-glucoside; 4-hydroxyphenyl-glucopyranoside; Hydroquinone-beta-D-glucoside; p-Hydroxyphenyl b-D-glucoside; p-Hydroxyphenyl β-D-glucoside; Arbutin, analytical standard; BJRNKVDFDLYUGJ-RMPHRYRLSA-N; Hydroquinone-D-glucoside; Arbutin (Uva, p-Arbutin); Hydroquinone-glucose; Hydroquinone glucose; Prestwick3_001026; Spectrum4_001474; ARBUTINUM [HPUS]; Spectrum5_000147; Spectrum3_001233; Spectrum2_000662; ARBUTIN [WHO-DD]; ARBUTIN [MART.]; ARBUTIN (MART.); Arbutin, >=98\\%; UNII-C5INA23HXF; ARBUTIN [HSDB]; ARBUTIN [INCI]; Tox21_111509_1; Uva,p-Arbutin; MEGxp0_001504; DivK1c_006410; BPBio1_001333; KBio2_006402; KBio3_002206; Tox21_111509; beta-Arbutin; KBio1_001354; Tox21_302428; ARBUTIN [MI]; KBio2_003834; KBio2_001266; SMP1_000028; C5INA23HXF; Arbutoside; Β-arbutin; b-Arbutin; p-Arbutin; Arbutinum; Arbutine; Ericolin; -Arbutin; Arbutyne; Arbutin; HYDRO H; Uvasol; Ursin; Ursi; 7OQ; 4-Hydroxyphenyl-β-D-glucopyranoside; Hydroquinone β-D-glucopyranoside; 4-Hydroxyphenyl hexopyranoside; Arbutin; Arbutin



数据库引用编号

37 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(1)

PlantCyc(0)

代谢反应

1 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(1)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

307 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 10 AKT1, BCL2, CASP3, CAT, MITF, NFE2L2, POMC, SIRT1, TYR, TYRP1
Golgi apparatus, trans-Golgi network membrane 1 LRBA
Peripheral membrane protein 1 GORASP1
Endosome membrane 1 TYRP1
Endoplasmic reticulum membrane 3 BCL2, HMOX1, LRBA
Nucleus 8 AKT1, BCL2, CASP3, HMOX1, MITF, MPO, NFE2L2, SIRT1
cytosol 11 AKT1, BCL2, CASP3, CAT, DCT, HMOX1, LIPE, LRBA, MITF, NFE2L2, SIRT1
centrosome 1 NFE2L2
nucleoplasm 7 AKT1, CASP3, HMOX1, MITF, MPO, NFE2L2, SIRT1
RNA polymerase II transcription regulator complex 1 NFE2L2
Cell membrane 4 AKT1, LIPE, LRBA, TNF
Cytoplasmic side 2 GORASP1, HMOX1
lamellipodium 1 AKT1
Golgi apparatus membrane 1 GORASP1
cell cortex 1 AKT1
cell surface 1 TNF
glutamatergic synapse 2 AKT1, CASP3
Golgi apparatus 3 GORASP1, LRBA, NFE2L2
Golgi membrane 2 GORASP1, INS
lysosomal membrane 3 GAA, LRBA, MITF
neuronal cell body 2 CASP3, TNF
postsynapse 1 AKT1
Cytoplasm, cytosol 2 LIPE, NFE2L2
Lysosome 3 GAA, MPO, TYR
plasma membrane 6 AKT1, DCT, GAA, LRBA, NFE2L2, TNF
Membrane 8 AKT1, BCL2, CAT, DCT, GAA, HMOX1, LIPE, LRBA
caveola 1 LIPE
extracellular exosome 3 CAT, GAA, MPO
Lysosome membrane 3 GAA, LRBA, MITF
endoplasmic reticulum 2 BCL2, HMOX1
extracellular space 6 HMOX1, IL6, INS, MPO, POMC, TNF
lysosomal lumen 1 GAA
perinuclear region of cytoplasm 2 HMOX1, TYR
mitochondrion 3 BCL2, CAT, SIRT1
protein-containing complex 4 AKT1, BCL2, CAT, MITF
intracellular membrane-bounded organelle 5 CAT, DCT, GAA, MPO, TYR
postsynaptic density 1 CASP3
chromatin silencing complex 1 SIRT1
Single-pass type I membrane protein 3 DCT, TYR, TYRP1
Secreted 4 GAA, IL6, INS, POMC
extracellular region 7 CAT, GAA, IL6, INS, MPO, POMC, TNF
Mitochondrion outer membrane 1 BCL2
Single-pass membrane protein 2 BCL2, LRBA
mitochondrial outer membrane 2 BCL2, HMOX1
mitochondrial matrix 1 CAT
Nucleus membrane 1 BCL2
Bcl-2 family protein complex 1 BCL2
nuclear membrane 1 BCL2
external side of plasma membrane 1 TNF
microtubule cytoskeleton 1 AKT1
nucleolus 1 SIRT1
Melanosome membrane 3 DCT, TYR, TYRP1
cell-cell junction 1 AKT1
Golgi-associated vesicle 1 TYR
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
vesicle 1 AKT1
heterochromatin 1 SIRT1
Membrane raft 1 TNF
pore complex 1 BCL2
focal adhesion 1 CAT
spindle 1 AKT1
cis-Golgi network 1 GORASP1
Peroxisome 1 CAT
intracellular vesicle 1 TYRP1
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
Nucleus, PML body 1 SIRT1
PML body 1 SIRT1
Mitochondrion intermembrane space 1 AKT1
mitochondrial intermembrane space 1 AKT1
secretory granule 2 MPO, POMC
nuclear inner membrane 1 SIRT1
ciliary basal body 1 AKT1
chromatin 3 MITF, NFE2L2, SIRT1
mediator complex 1 NFE2L2
phagocytic cup 1 TNF
fibrillar center 1 SIRT1
nuclear envelope 1 SIRT1
endosome lumen 1 INS
Lipid droplet 1 LIPE
Membrane, caveola 1 LIPE
tertiary granule membrane 1 GAA
Melanosome 3 DCT, TYR, TYRP1
euchromatin 1 SIRT1
myelin sheath 1 BCL2
azurophil granule 1 MPO
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 3 CAT, INS, POMC
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 IL6, INS
transport vesicle 1 INS
azurophil granule membrane 1 GAA
azurophil granule lumen 1 MPO
Endoplasmic reticulum-Golgi intermediate compartment membrane 2 GORASP1, INS
Golgi apparatus, cis-Golgi network membrane 1 GORASP1
Single-pass type IV membrane protein 1 HMOX1
clathrin-coated endocytic vesicle membrane 1 TYRP1
phagocytic vesicle lumen 1 MPO
protein-DNA complex 1 NFE2L2
ficolin-1-rich granule membrane 1 GAA
death-inducing signaling complex 1 CASP3
eNoSc complex 1 SIRT1
rDNA heterochromatin 1 SIRT1
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
catalase complex 1 CAT
interleukin-6 receptor complex 1 IL6
autolysosome lumen 1 GAA
BAD-BCL-2 complex 1 BCL2
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF
[SirtT1 75 kDa fragment]: Cytoplasm 1 SIRT1


文献列表

  • Simón Miranda, Marion Koop, Andrea Angeli, Jorge Lagrèze, Mickael Malnoy, Stefan Martens. Assessment and Partial Characterization of Candidate Genes in Dihydrochalcone and Arbutin Biosynthesis in an Apple-Pear Hybrid by De Novo Transcriptome Assembly. Journal of agricultural and food chemistry. 2024 May; 72(20):11804-11819. doi: 10.1021/acs.jafc.4c01006. [PMID: 38717061]
  • Peng Shu, Yuan Wang, Lanyue Zhang. The Effect of α-Arbutin on UVB-Induced Damage and Its Underlying Mechanism. Molecules (Basel, Switzerland). 2024 Apr; 29(9):. doi: 10.3390/molecules29091921. [PMID: 38731413]
  • Oguzhan Birdal, Irmak Ferah Okkay, Ufuk Okkay, Cemil Bayram, Behzad Mokthare, Muhammed Sait Ertugrul, Ahmet Hacimuftuoglu, Emrah Aksakal, Yavuzer Koza, Mehmet Saygi, Huseyin Senocak. Protective effects of arbutin against doxorubicin-induced cardiac damage. Molecular biology reports. 2024 Apr; 51(1):532. doi: 10.1007/s11033-024-09488-4. [PMID: 38637360]
  • Mohammad Saleh Bahreini, Seyyed Farzad Pourmohammadi, Meysam Gholami, Mojtaba Habibollahi, Ardalan Pasdaran, Azadeh Hamedi, Qasem Asgari. Anti-Toxoplasma In Vitro and In Vivo Activity of Pyrus boissieriana Arbutin-Rich Fraction. Acta parasitologica. 2024 Mar; 69(1):567-573. doi: 10.1007/s11686-023-00759-x. [PMID: 38231312]
  • Boxiao Wu, Churan Li, Huan Kan, Yingjun Zhang, Xiaoping Rao, Yun Liu, Ping Zhao. Hypolipidemic and Antithrombotic Effect of 6'-O-Caffeoylarbutin from Vaccinium dunalianum Based on Zebrafish Model, Network Pharmacology, and Molecular Docking. Molecules (Basel, Switzerland). 2024 Feb; 29(4):. doi: 10.3390/molecules29040780. [PMID: 38398534]
  • Dong Xie, Wengan Fu, Tiantian Yuan, Kangjia Han, Yuxiu Lv, Qi Wang, Qian Jiang, Yingjun Zhang, Guolei Zhu, Junming Xu, Ping Zhao, Xiaoqin Yang. 6'-O-Caffeoylarbutin from Quezui Tea: A Highly Effective and Safe Tyrosinase Inhibitor. International journal of molecular sciences. 2024 Jan; 25(2):. doi: 10.3390/ijms25020972. [PMID: 38256044]
  • Yi-Chi Chen, Yang-Yang Liu, Liqiang Chen, Dong-Mei Tang, YunLi Zhao, Xiao-Dong Luo. Antimelanogenic Effect of Isoquinoline Alkaloids from Plumula Nelumbinis. Journal of agricultural and food chemistry. 2023 Nov; 71(43):16090-16101. doi: 10.1021/acs.jafc.3c03784. [PMID: 37856847]
  • Samuel D Zarfos, Bianca J Deans, Curtis C Ho, Gregory J Jordan, Jason A Smith, Alex C Bissember. Distinctive Arbutin-Containing Markers: Chemotaxonomic Significance and Insights into the Evolution of Proteaceae Phytochemistry. Chemistry & biodiversity. 2023 Nov; 20(11):e202301112. doi: 10.1002/cbdv.202301112. [PMID: 37726205]
  • Cinzia Sanna, Ilaria Chiocchio, Manuela Mandrone, Francesca Bonvicini, Giovanna A Gentilomi, Simona Trincia, Ferruccio Poli. Metabolomic analysis and bioactivities of Arbutus unedo leaves harvested across the seasons in different natural habitats of Sardinia (Italy). BMC plant biology. 2023 Oct; 23(1):490. doi: 10.1186/s12870-023-04497-0. [PMID: 37828439]
  • Silvia Yunmam, Hae Ran Lee, Seong Min Hong, Ji-Young Kim, Tong Ho Kang, Ai Young Lee, Dae Sik Jang, Sun Yeou Kim. Aspacochioside C from Asparagus cochinchinensis attenuates eumelanin synthesis via inhibition of TRP2 expression. Scientific reports. 2023 09; 13(1):14831. doi: 10.1038/s41598-023-41248-5. [PMID: 37684311]
  • Ning An, Shubin Zhou, Xin Chen, Jia Wang, Xinxiao Sun, Xiaolin Shen, Qipeng Yuan. High-yield production of β-arbutin by identifying and eliminating byproducts formation. Applied microbiology and biotechnology. 2023 Aug; ?(?):. doi: 10.1007/s00253-023-12706-x. [PMID: 37597019]
  • Yujuan Shen, Yuanyuan Xia, Xianzhong Chen. Research progress and application of enzymatic synthesis of glycosyl compounds. Applied microbiology and biotechnology. 2023 Jul; ?(?):. doi: 10.1007/s00253-023-12652-8. [PMID: 37428188]
  • Zhengming Xu, Shuang Liu, Huining Lai, Lijun You, Zhengang Zhao. Green-Efficient Enzymatic Synthesis and Characterization of Liposoluble 6'/6″-O-Lauryl Phenolic Glycosides with Enhanced Intestinal Permeability. Journal of agricultural and food chemistry. 2023 May; 71(20):7689-7702. doi: 10.1021/acs.jafc.3c00527. [PMID: 37167604]
  • Elif Ayazoglu Demir, Selim Demir, Ilke Onur Kazaz, Hatice Kucuk, Nihal Turkmen Alemdar, Ali Buyuk, Ahmet Mentese, Yuksel Aliyazicioglu. Arbutin abrogates testicular ischemia/reperfusion injury in rats through repression of inflammation and ER stress. Tissue & cell. 2023 Mar; 82(?):102056. doi: 10.1016/j.tice.2023.102056. [PMID: 36921493]
  • H Turan Akkoyun, Ahmet Uyar, Mahire Bayramoglu Akkoyun, Aydın Şükrü Bengü, Şule Melek, Fatma Karagözoğlu, Sevinç Aydın, Suat Ekin, Sinem Aslan Erdem. The protective effect of arbutin against potassium bromate-induced oxidative damage in the rat brain. Journal of biochemical and molecular toxicology. 2023 Feb; 37(2):e23248. doi: 10.1002/jbt.23248. [PMID: 36284482]
  • Jin-Han Yang, Tong-Chen Bai, Lu-Li Shi, Bo Hou, Ran Tang, Rong-Ping Zhang, Xing-Long Chen. Antihyperlipidemic effect of Vaccinium dunalianum buds based on biological activity screening and LC-MS. Journal of ethnopharmacology. 2023 Jan; 306(?):116190. doi: 10.1016/j.jep.2023.116190. [PMID: 36693548]
  • Lutfun Nahar, Afaf Al-Groshi, Anil Kumar, Satyajit D Sarker. Arbutin: Occurrence in Plants, and Its Potential as an Anticancer Agent. Molecules (Basel, Switzerland). 2022 Dec; 27(24):. doi: 10.3390/molecules27248786. [PMID: 36557918]
  • Danni Feng, Zhongxiang Fang, Pangzhen Zhang. The melanin inhibitory effect of plants and phytochemicals: A systematic review. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2022 Dec; 107(?):154449. doi: 10.1016/j.phymed.2022.154449. [PMID: 36126406]
  • Kun Zhou, Dingyan Lu, Jingrui You, Ting Liu, Jia Sun, Yuan Lu, Jie Pan, Yongjun Li, Chunhua Liu. Integrated plasma pharmacochemistry and network pharmacology to explore the mechanism of Gerberae Piloselloidis Herba in treatment of allergic asthma. Journal of ethnopharmacology. 2022 Nov; 298(?):115624. doi: 10.1016/j.jep.2022.115624. [PMID: 35970314]
  • Chunhua Liu, Jingrui You, Kun Zhou, Zipeng Gong, Jie Pan, Jia Sun, Ting Liu, Aimin Wang, Yonglin Wang, Yuan Lu, Yongjun Li. Comparative pharmacokinetics of 11 components from the active part of Gerberae Piloselloidis Herba after oral administration in control and asthmatic mice. Journal of separation science. 2022 Nov; 45(22):4023-4038. doi: 10.1002/jssc.202101010. [PMID: 36070105]
  • Shubhadeep Roychoudhury, Dipika Das, Sandipan Das, Niraj Kumar Jha, Mahadeb Pal, Adriana Kolesarova, Kavindra Kumar Kesari, Jogen C Kalita, Petr Slama. Clinical Potential of Himalayan Herb Bergenia ligulata: An Evidence-Based Study. Molecules (Basel, Switzerland). 2022 Oct; 27(20):. doi: 10.3390/molecules27207039. [PMID: 36296631]
  • Jingang He, Yunxiao Feng, Yudou Cheng, Thirupathi Karuppanapandian, Jinxiao Wang, Junfeng Guan. Changes in α-Farnesene and Phenolic Metabolism and the Expression of Associated Genes during the Development of Superficial Scald in Two Distinct Pear Cultivars. International journal of molecular sciences. 2022 Oct; 23(20):. doi: 10.3390/ijms232012088. [PMID: 36292939]
  • Linxuan Zhang, Yue Ren, Fanli Meng, Hangbin Bao, Fei Xing, Chengming Tian. Verification of the Protective Effects of Poplar Phenolic Compounds Against Poplar Anthracnose. Phytopathology. 2022 Oct; 112(10):2198-2206. doi: 10.1094/phyto-12-21-0509-r. [PMID: 35578737]
  • Yong-Peng Wang, Yu-Dan Wang, Ya-Ping Liu, Jian-Xin Cao, Mei-Lian Yang, Yi-Fen Wang, Afsar Khan, Tian-Rui Zhao, Gui-Guang Cheng. 6'-O-Caffeoylarbutin from Que Zui tea ameliorates acetaminophen-induced liver injury via enhancing antioxidant ability and regulating the PI3K signaling pathway. Food & function. 2022 May; 13(9):5299-5316. doi: 10.1039/d2fo00507g. [PMID: 35441652]
  • Ana Huđek Turković, Marija Gunjača, Marko Marjanović, Marija Lovrić, Ana Butorac, Dubravka Rašić, Maja Peraica, Valerija Vujčić Bok, Ivana Šola, Gordana Rusak, Ksenija Durgo. Proteome changes in human bladder T24 cells induced by hydroquinone derived from Arctostaphylos uva-ursi herbal preparation. Journal of ethnopharmacology. 2022 May; 289(?):115092. doi: 10.1016/j.jep.2022.115092. [PMID: 35143933]
  • Piotr Sugier, Łukasz Sęczyk, Danuta Sugier. Variation in Population and Solvents as Factors Determining the Chemical Composition and Antioxidant Potential of Arctostaphylos uva-ursi (L.) Spreng. Leaf Extracts. Molecules (Basel, Switzerland). 2022 Mar; 27(7):. doi: 10.3390/molecules27072247. [PMID: 35408643]
  • Jingjing Tan, Manoj Kumar Yadav, Sushma Devi, Manish Kumar. Neuroprotective effects of arbutin against oxygen and glucose deprivation-induced oxidative stress and neuroinflammation in rat cortical neurons. Acta pharmaceutica (Zagreb, Croatia). 2022 Mar; 72(1):123-134. doi: 10.2478/acph-2022-0002. [PMID: 36651531]
  • Vesna Benković, Nives Marčina, Anica Horvat Knežević, Dunja Šikić, Vedran Rajevac, Mirta Milić, Nevenka Kopjar. Potential radioprotective properties of arbutin against ionising radiation on human leukocytes in vitro. Mutation research. Genetic toxicology and environmental mutagenesis. 2021 Dec; 872(?):503413. doi: 10.1016/j.mrgentox.2021.503413. [PMID: 34798933]
  • Mohammad F Bostanudin, Aisha Salam, Arshad Mahmood, Mosab Arafat, Amirah N Kaharudin, Shariza Sahudin, Azwan Mat Lazim, Ahmad Azfaralariff. Formulation and In-Vitro Characterisation of Cross-Linked Amphiphilic Guar Gum Nanocarriers for Percutaneous Delivery of Arbutin. Journal of pharmaceutical sciences. 2021 12; 110(12):3907-3918. doi: 10.1016/j.xphs.2021.08.014. [PMID: 34403653]
  • Chuan Zhang, Huiping Zhu, Hui Jie, Hengyue Ding, Hongwen Sun. Arbutin ameliorated ulcerative colitis of mice induced by dextran sodium sulfate (DSS). Bioengineered. 2021 12; 12(2):11707-11715. doi: 10.1080/21655979.2021.2005746. [PMID: 34783296]
  • Chun-Wei Wang, Ming-Chen Chuang, Chieh-Yi Chang, Chien-Hsiang Chang, Yu-Min Yang. Stable Ethosome-like Catanionic Vesicles for Transdermal Hydrophilic Drug Delivery with Predictable Encapsulation Efficiency. Journal of oleo science. 2021 Oct; 70(10):1391-1401. doi: 10.5650/jos.ess21072. [PMID: 34497178]
  • Rongsheng Wang, Jinji Mu. Arbutin attenuates ethanol-induced acute hepatic injury by the modulation of oxidative stress and Nrf-2/HO-1 signaling pathway. Journal of biochemical and molecular toxicology. 2021 Oct; 35(10):e22872. doi: 10.1002/jbt.22872. [PMID: 34346143]
  • Narges Soltani Ghofrani, Maedeh Sheikhi, Javad Zamani Amirzakaria, Sorour Hassani, Saeed Aminzadeh, Kamahldin Haghbeen. New Insight into the Interactions of Arbutin with Mushroom Tyrosinase. The protein journal. 2021 10; 40(5):689-698. doi: 10.1007/s10930-021-10004-x. [PMID: 34047882]
  • Xue-Chao Song, Elena Canellas, Nicola Dreolin, Cristina Nerin, Jeff Goshawk. Discovery and Characterization of Phenolic Compounds in Bearberry (Arctostaphylos uva-ursi) Leaves Using Liquid Chromatography-Ion Mobility-High-Resolution Mass Spectrometry. Journal of agricultural and food chemistry. 2021 Sep; 69(37):10856-10868. doi: 10.1021/acs.jafc.1c02845. [PMID: 34493038]
  • Zhangkai Yang, Hangyu Shi, Arunachalam Chinnathambi, Saleh H Salmen, Sulaiman A Alharbi, Vishnu Priya Veeraraghavan, Krishna Mohan Surapaneni, Palanisamy Arulselvan. Arbutin exerts anticancer activity against rat C6 glioma cells by inducing apoptosis and inhibiting the inflammatory markers and P13/Akt/mTOR cascade. Journal of biochemical and molecular toxicology. 2021 Sep; 35(9):e22857. doi: 10.1002/jbt.22857. [PMID: 34338399]
  • Majid Saeedi, Khadijeh Khezri, Abbas Seyed Zakaryaei, Hassan Mohammadamini. A comprehensive review of the therapeutic potential of α-arbutin. Phytotherapy research : PTR. 2021 Aug; 35(8):4136-4154. doi: 10.1002/ptr.7076. [PMID: 33724594]
  • Md Shaekh Forid, Md Atiar Rahman, Mohd Fadhlizil Fasihi Mohd Aluwi, Md Nazim Uddin, Tapashi Ghosh Roy, Milon Chandra Mohanta, Akm Moyeenul Huq, Zainul Amiruddin Zakaria. Pharmacoinformatics and UPLC-QTOF/ESI-MS-Based Phytochemical Screening of Combretum indicum against Oxidative Stress and Alloxan-Induced Diabetes in Long-Evans Rats. Molecules (Basel, Switzerland). 2021 Jul; 26(15):. doi: 10.3390/molecules26154634. [PMID: 34361788]
  • Onkar Bedi, Niharika Srivastava, Davinder Parsad, Pawan Krishan. Fatty acid synthase inhibition ameliorates diabetes induced liver injury in rodent experimental model. European journal of pharmacology. 2021 Jun; 901(?):174078. doi: 10.1016/j.ejphar.2021.174078. [PMID: 33839087]
  • Aryana Radmard, Majid Saeedi, Katayoun Morteza-Semnani, Seyyed Mohammad Hassan Hashemi, Ali Nokhodchi. An eco-friendly and green formulation in lipid nanotechnology for delivery of a hydrophilic agent to the skin in the treatment and management of hyperpigmentation complaints: Arbutin niosome (Arbusome). Colloids and surfaces. B, Biointerfaces. 2021 May; 201(?):111616. doi: 10.1016/j.colsurfb.2021.111616. [PMID: 33618082]
  • Chaoting Ma, Dandan Zhang, Qiuyan Ma, Yu Liu, Yingxin Yang. Arbutin inhibits inflammation and apoptosis by enhancing autophagy via SIRT1. Advances in clinical and experimental medicine : official organ Wroclaw Medical University. 2021 May; 30(5):535-544. doi: 10.17219/acem/133493. [PMID: 33974755]
  • Şevki Adem, Volkan Eyupoglu, Iqra Sarfraz, Azhar Rasul, Ameer Fawad Zahoor, Muhammad Ali, Mohnad Abdalla, Ibrahim M Ibrahim, Abdo A Elfiky. Caffeic acid derivatives (CAFDs) as inhibitors of SARS-CoV-2: CAFDs-based functional foods as a potential alternative approach to combat COVID-19. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2021 May; 85(?):153310. doi: 10.1016/j.phymed.2020.153310. [PMID: 32948420]
  • Tianrui Zhao, Mengxue Sun, Lingpeng Kong, Qingwang Xue, Yudan Wang, Yifen Wang, Afsar Khan, Jianxin Cao, Guiguang Cheng. Bioactivity-Guided Isolation of Phytochemicals from Vaccinium dunalianum Wight and Their Antioxidant and Enzyme Inhibitory Activities. Molecules (Basel, Switzerland). 2021 Apr; 26(7):. doi: 10.3390/molecules26072075. [PMID: 33916551]
  • Beibei Zhang, Mengnan Zeng, Benke Li, Yuxuan Kan, Shengchao Wang, Bing Cao, Yanjie Huang, Xiaoke Zheng, Weisheng Feng. Arbutin attenuates LPS-induced acute kidney injury by inhibiting inflammation and apoptosis via the PI3K/Akt/Nrf2 pathway. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2021 Feb; 82(?):153466. doi: 10.1016/j.phymed.2021.153466. [PMID: 33494001]
  • S Sivasangari, L Asaikumar, L Vennila. Arbutin prevents alterations in mitochondrial and lysosomal enzymes in isoproterenol-induced myocardial infarction: An in vivo study. Human & experimental toxicology. 2021 Jan; 40(1):100-112. doi: 10.1177/0960327120945790. [PMID: 32757845]
  • Haoran Guo, Hongliang Zeng, Chuhan Fu, Jinhua Huang, Jianyun Lu, Yibo Hu, Ying Zhou, Liping Luo, Yushan Zhang, Lan Zhang, Jing Chen, Qinghai Zeng. Identification of Sitogluside as a Potential Skin-Pigmentation-Reducing Agent through Network Pharmacology. Oxidative medicine and cellular longevity. 2021; 2021(?):4883398. doi: 10.1155/2021/4883398. [PMID: 34603597]
  • Cheng-Qun Wang, Xiu-Mei Wang, Bing-Liang Li, Yuan-Min Zhang, Lei Wang. Arbutin suppresses osteosarcoma progression via miR-338-3p/MTHFD1L and inactivation of the AKT/mTOR pathway. FEBS open bio. 2021 01; 11(1):289-299. doi: 10.1002/2211-5463.13024. [PMID: 33146000]
  • Vanessa Cristina de Carvalho Braga, Gérson Antônio Pianetti, Isabela Costa César. Comparative stability of arbutin in Arctostaphylos uva-ursi by a new comprehensive stability-indicating HPLC method. Phytochemical analysis : PCA. 2020 Nov; 31(6):884-891. doi: 10.1002/pca.2953. [PMID: 32495959]
  • Onkar Bedi, Savera Aggarwal, Nirupma Trehanpati, Gayatri Ramakrishna, Ajmer Singh Grewal, Pawan Krishan. In vitro targeted screening and molecular docking of stilbene, quinones, and flavonoid on 3T3-L1 pre-adipocytes for anti-adipogenic actions. Naunyn-Schmiedeberg's archives of pharmacology. 2020 11; 393(11):2093-2106. doi: 10.1007/s00210-020-01919-w. [PMID: 32588069]
  • Karlo Jurica, Vesna Benković, Sunčana Sikirić, Irena Brčić Karačonji, Nevenka Kopjar. The effects of strawberry tree (Arbutus unedo L.) water leaf extract and arbutin upon kidney function and primary DNA damage in renal cells of rats. Natural product research. 2020 Aug; 34(16):2354-2357. doi: 10.1080/14786419.2018.1534106. [PMID: 30417709]
  • Nasiruddin Nalban, Rajendra Sangaraju, Sateesh Alavala, Salma Mukhtar Mir, Mahesh Kumar Jerald, Ramakrishna Sistla. Arbutin Attenuates Isoproterenol-Induced Cardiac Hypertrophy by Inhibiting TLR-4/NF-κB Pathway in Mice. Cardiovascular toxicology. 2020 06; 20(3):235-248. doi: 10.1007/s12012-019-09548-3. [PMID: 31485892]
  • Yaqi Ding, Deqin Kong, Tong Zhou, Nai-di Yang, Chenqi Xin, Jiajia Xu, Qi Wang, Hang Zhang, Qiong Wu, Xiaomei Lu, Kahleong Lim, Bo Ma, Chengwu Zhang, Lin Li, Wei Huang. α-Arbutin Protects Against Parkinson's Disease-Associated Mitochondrial Dysfunction In Vitro and In Vivo. Neuromolecular medicine. 2020 03; 22(1):56-67. doi: 10.1007/s12017-019-08562-6. [PMID: 31401719]
  • Karlo Jurica, Vesna Benković, Sunčana Sikirić, Nevenka Kopjar, Irena Brčić Karačonji. Liver function and DNA integrity in hepatocytes of rats evaluated after treatments with strawberry tree (Arbutus unedo L.) water leaf extract and arbutin. Drug and chemical toxicology. 2020 Mar; 43(2):127-137. doi: 10.1080/01480545.2018.1477794. [PMID: 29874937]
  • Kazuma Katsutani, Sachiko Sugimoto, Yoshi Yamano, Hideaki Otsuka, Katsuyoshi Matsunami, Tsutomu Mizuta. Eudesmane-type sesquiterpene glycosides: sonneratiosides A-E and eudesmol β-D-glucopyranoside from the leaves of Sonneratia alba. Journal of natural medicines. 2020 Jan; 74(1):119-126. doi: 10.1007/s11418-019-01353-0. [PMID: 31392565]
  • Bettina Rainer, Silvia Revoltella, Fabian Mayr, Julia Moesslacher, Valentina Scalfari, Roland Kohl, Birgit Waltenberger, Konrad Pagitz, Bianka Siewert, Stefan Schwaiger, Hermann Stuppner. From bench to counter: Discovery and validation of a peony extract as tyrosinase inhibiting cosmeceutical. European journal of medicinal chemistry. 2019 Dec; 184(?):111738. doi: 10.1016/j.ejmech.2019.111738. [PMID: 31655335]
  • Anis I Anwar, Siswanto Wahab, Widya Widita, Airin R Nurdin, Suci Budhiani, Arifin Seweng. Randomized control trial outcomes of tranexamic acid combination serum as a depigmenting agent for the use in healthy individuals. Dermatologic therapy. 2019 11; 32(6):e13146. doi: 10.1111/dth.13146. [PMID: 31664751]
  • Zohreh Dastan, Mahdi Pouramir, Maryam Ghasemi-Kasman, Zahra Ghasemzadeh, Masoumeh Dadgar, Mohammad Gol, Manouchehr Ashrafpour, Mohsen Pourghasem, Ali Akbar Moghadamnia, Soraya Khafri. Arbutin reduces cognitive deficit and oxidative stress in animal model of Alzheimer's disease. The International journal of neuroscience. 2019 Nov; 129(11):1145-1153. doi: 10.1080/00207454.2019.1638376. [PMID: 31251091]
  • Denilson F Oliveira, Viviane A Costa, Willian C Terra, Vicente P Campos, Pacelli M Paula, Samuel J Martins. Impact of phenolic compounds on Meloidogyne incognita in vitro and in tomato plants. Experimental parasitology. 2019 Apr; 199(?):17-23. doi: 10.1016/j.exppara.2019.02.009. [PMID: 30790574]
  • Jie Zhang, Toshihiro Akihisa, Masahiro Kurita, Takashi Kikuchi, Wan-Fang Zhu, Feng Ye, Zhen-Huan Dong, Wen-Yuan Liu, Feng Feng, Jian Xu. Melanogenesis-Inhibitory and Cytotoxic Activities of Triterpene Glycoside Constituents from the Bark of Albizia procera. Journal of natural products. 2018 12; 81(12):2612-2620. doi: 10.1021/acs.jnatprod.8b00167. [PMID: 30520635]
  • Min-Chi Cheng, Tzong-Huei Lee, Yi-Tzu Chu, Li-Ling Syu, Su-Jung Hsu, Chia-Hsiung Cheng, Jender Wu, Ching-Kuo Lee. Melanogenesis Inhibitors from the Rhizoma of Ligusticum Sinense in B16-F10 Melanoma Cells In Vitro and Zebrafish In Vivo. International journal of molecular sciences. 2018 Dec; 19(12):. doi: 10.3390/ijms19123994. [PMID: 30545008]
  • Sohrab N Ali, Thamara K Dayarathna, Aymon N Ali, Tijani Osumah, Mohamed Ahmed, Tyler T Cooper, Nicholas E Power, Dongxing Zhang, Dajung Kim, Rachel Kim, Andre St Amant, Jinqiang Hou, Thomas Tailly, Jun Yang, Len Luyt, Paul A Spagnuolo, Jeremy P Burton, Hassan Razvi, Hon S Leong. Drosophila melanogaster as a function-based high-throughput screening model for antinephrolithiasis agents in kidney stone patients. Disease models & mechanisms. 2018 11; 11(11):. doi: 10.1242/dmm.035873. [PMID: 30082495]
  • Songwei Wang, Cong Fu, Muhammad Bilal, Hongbo Hu, Wei Wang, Xuehong Zhang. Enhanced biosynthesis of arbutin by engineering shikimate pathway in Pseudomonas chlororaphis P3. Microbial cell factories. 2018 Nov; 17(1):174. doi: 10.1186/s12934-018-1022-8. [PMID: 30414616]
  • Ning Zhou, Meng-Nan Zeng, Kai Li, Yan-Yun Yang, Zhi-Yao Bai, Xiao-Ke Zheng, Wei-Sheng Feng. An integrated metabolomic strategy for the characterization of the effects of Chinese yam and its three active components on septic cardiomyopathy. Food & function. 2018 Sep; 9(9):4989-4997. doi: 10.1039/c8fo00688a. [PMID: 30187904]
  • Claudio Frezza, Alessandro Venditti, Giorgia Matrone, Ilaria Serafini, Sebastiano Foddai, Armandodoriano Bianco, Mauro Serafini. Iridoid glycosides and polyphenolic compounds from Teucrium chamaedrys L. Natural product research. 2018 Jul; 32(13):1583-1589. doi: 10.1080/14786419.2017.1392948. [PMID: 29058476]
  • Bianca J Deans, Nathan L Kilah, Gregory J Jordan, Alex C Bissember, Jason A Smith. Arbutin Derivatives Isolated from Ancient Proteaceae: Potential Phytochemical Markers Present in Bellendena, Cenarrhenes, and Persoonia Genera. Journal of natural products. 2018 05; 81(5):1241-1251. doi: 10.1021/acs.jnatprod.7b01038. [PMID: 29715019]
  • Qinghao Jin, Xiang Hua Han, Cheong-Yong Yun, Chul Lee, Jin Woo Lee, Dongho Lee, Mi Kyeong Lee, Sang-Hun Jung, Jin Tae Hong, Youngsoo Kim, Bang Yeon Hwang. Melanogenesis inhibitory pregnane glycosides from Cynanchum atratum. Bioorganic & medicinal chemistry letters. 2018 04; 28(7):1252-1256. doi: 10.1016/j.bmcl.2018.01.004. [PMID: 29526485]
  • Karlo Jurica, Irena Brčić Karačonji, Nevenka Kopjar, Ana Shek-Vugrovečki, Tihana Cikač, Vesna Benković. The effects of strawberry tree water leaf extract, arbutin and hydroquinone on haematological parameters and levels of primary DNA damage in white blood cells of rats. Journal of ethnopharmacology. 2018 Apr; 215(?):83-90. doi: 10.1016/j.jep.2017.12.039. [PMID: 29288828]
  • Hee-Young Ahn, Young-Moo Choo, Young-Su Cho. Anti-Pigmentation Effects of Eight Phellinus linteus-Fermented Traditional Crude Herbal Extracts on Brown Guinea Pigs of Ultraviolet B-Induced Hyperpigmentation. Journal of microbiology and biotechnology. 2018 Mar; 28(3):375-380. doi: 10.4014/jmb.1711.11043. [PMID: 29316744]
  • Liyan Jiang, Di Wang, Yongfeng Zhang, Junyang Li, Zhiping Wu, Zhi Wang, Di Wang. Investigation of the pro-apoptotic effects of arbutin and its acetylated derivative on murine melanoma cells. International journal of molecular medicine. 2018 Feb; 41(2):1048-1054. doi: 10.3892/ijmm.2017.3256. [PMID: 29207077]
  • Mengnan Zeng, Li Zhang, Miao Li, Beibei Zhang, Ning Zhou, Yingying Ke, Weisheng Feng, Xiaoke Zheng. Estrogenic Effects of the Extracts from the Chinese Yam (Dioscorea opposite Thunb.) and Its Effective Compounds in Vitro and in Vivo. Molecules (Basel, Switzerland). 2018 Jan; 23(2):. doi: 10.3390/molecules23020011. [PMID: 29360751]
  • Li-Yan Song, Fang Huang, Yan Wang, Zu-Jian Wu, Ming-An Ouyang. New Alkaloid and Aromatic Glucoside from the Flowers of Cymbidium Lunagrad Eternal Green. Molecules (Basel, Switzerland). 2018 Jan; 23(1):. doi: 10.3390/molecules23010099. [PMID: 29301372]
  • Na Li, Wei-Lin Zeng, Xu-Lu Luo, Chong-Ren Yang, Ying-Jun Zhang, Yong Ding, Ping Zhao. A new arbutin derivative from the leaves of Vaccinium dunalianum wight. Natural product research. 2018 Jan; 32(1):65-70. doi: 10.1080/14786419.2017.1333993. [PMID: 28595463]
  • Yoshiaki Manse, Kiyofumi Ninomiya, Ryosuke Nishi, Yoshinori Hashimoto, Saowanee Chaipech, Osamu Muraoka, Toshio Morikawa. Labdane-Type Diterpenes, Galangalditerpenes A-C, with Melanogenesis Inhibitory Activity from the Fruit of Alpinia galanga. Molecules (Basel, Switzerland). 2017 Dec; 22(12):. doi: 10.3390/molecules22122279. [PMID: 29261124]
  • Elizabeth Vaca, Claire Behrens, Tiju Theccanat, Jun-Yong Choe, John V Dean. Mechanistic differences in the uptake of salicylic acid glucose conjugates by vacuolar membrane-enriched vesicles isolated from Arabidopsis thaliana. Physiologia plantarum. 2017 Nov; 161(3):322-338. doi: 10.1111/ppl.12602. [PMID: 28665551]
  • Beata Żbikowska, Roman Franiczek, Alina Sowa, Grażyna Połukord, Barbara Krzyżanowska, Zbigniew Sroka. Antimicrobial and Antiradical Activity of Extracts Obtained from Leaves of Five Species of the Genus Bergenia: Identification of Antimicrobial Compounds. Microbial drug resistance (Larchmont, N.Y.). 2017 Sep; 23(6):771-780. doi: 10.1089/mdr.2016.0251. [PMID: 28118088]
  • Xiaolin Shen, Jia Wang, Jian Wang, Zhenya Chen, Qipeng Yuan, Yajun Yan. High-level De novo biosynthesis of arbutin in engineered Escherichia coli. Metabolic engineering. 2017 07; 42(?):52-58. doi: 10.1016/j.ymben.2017.06.001. [PMID: 28583673]
  • Lenka Tůmová, Iva Dolečková, Helena Hendrychová, Marie Kašparová. Arbutin Content and Tyrosinase Activity of Bergenia Extracts. Natural product communications. 2017 Apr; 12(4):549-552. doi: ". [PMID: 30520594]
  • Namrita Lall, Elizabeth Mogapi, Marco Nuno de Canha, Bridget Crampton, Mabatho Nqephe, Ahmed A Hussein, Vivek Kumar. Insights into tyrosinase inhibition by compounds isolated from Greyia radlkoferi Szyszyl using biological activity, molecular docking and gene expression analysis. Bioorganic & medicinal chemistry. 2016 11; 24(22):5953-5959. doi: 10.1016/j.bmc.2016.09.054. [PMID: 27720556]
  • Kazuya Hagiwara, Masae Okura, Yasuyuki Sumikawa, Tokimasa Hida, Atsushi Kuno, Yoshiyuki Horio, Toshiharu Yamashita. Biochemical effects of the flavanol-rich lychee fruit extract on the melanin biosynthesis and reactive oxygen species. The Journal of dermatology. 2016 Oct; 43(10):1174-1183. doi: 10.1111/1346-8138.13326. [PMID: 26970333]
  • Wei-Yan Qi, Na Ou, Xiao-Dong Wu, Han-Mei Xu. New arbutin derivatives from the leaves of Heliciopsis lobata with cytotoxicity. Chinese journal of natural medicines. 2016 Oct; 14(10):789-793. doi: 10.1016/s1875-5364(16)30094-2. [PMID: 28236409]
  • Noelani Gonzalez, Maritza Perez. Natural Cosmeceutical Ingredients for Hyperpigmentation. Journal of drugs in dermatology : JDD. 2016 Jan; 15(1):26-34. doi: . [PMID: 26741379]
  • Luyan Zhang, Wei Zhang, Gang Chen. Determination of arbutin and bergenin in Bergeniae Rhizoma by capillary electrophoresis with a carbon nanotube-epoxy composite electrode. Journal of pharmaceutical and biomedical analysis. 2015 Nov; 115(?):323-9. doi: 10.1016/j.jpba.2015.07.044. [PMID: 26263060]
  • Jian Wang, Yang-min Ma, Meng-ru Yan, Qian Xu, Zi-rui Qu, Zhi Miao. [Chemical Compositions from Stems and Branches of Sorbaria arborea]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2015 Oct; 38(10):2098-101. doi: . [PMID: 27254923]
  • Dong-Yang Zhang, Xiao-Hui Yao, Ming-Hui Duan, Meng Luo, Chun-Jian Zhao, Yuan-Gang Zu, Yu-Jie Fu. An effective homogenate-assisted negative pressure cavitation extraction for the determination of phenolic compounds in pyrola by LC-MS/MS and the evaluation of its antioxidant activity. Food & function. 2015 Oct; 6(10):3323-33. doi: 10.1039/c5fo00727e. [PMID: 26256648]
  • Dejan Gođevac, Jovana Stanković, Miroslav Novaković, Boban Anđelković, Zora Dajić-Stevanović, Milica Petrović, Miroslava Stanković. Phenolic Compounds from Atriplex littoralis and Their Radiation-Mitigating Activity. Journal of natural products. 2015 Sep; 78(9):2198-204. doi: 10.1021/acs.jnatprod.5b00273. [PMID: 26290401]
  • Karlo Jurica, Irena Brčić Karačonji, Sandra Šegan, Dušanka Milojković Opsenica, Dario Kremer. Quantitative analysis of arbutin and hydroquinone in strawberry tree (Arbutus unedo L., Ericaceae) leaves by gas chromatography-mass spectrometry. Arhiv za higijenu rada i toksikologiju. 2015 Sep; 66(3):197-202. doi: 10.1515/aiht-2015-66-2696. [PMID: 26444340]
  • Monika Morag, Joanna Nawrot, Idzi Siatkowski, Zygmunt Adamski, Tomasz Fedorowicz, Renata Dawid-Pac, Maria Urbanska, Gerard Nowak. A double-blind, placebo-controlled randomized trial of Serratulae quinquefoliae folium, a new source of β-arbutin, in selected skin hyperpigmentations. Journal of cosmetic dermatology. 2015 Sep; 14(3):185-90. doi: 10.1111/jocd.12147. [PMID: 26119285]
  • Genzoh Tanabe, Youta Sugano, Miki Shirato, Naoki Sonoda, Nozomi Tsutsui, Toshio Morikawa, Kiyofumi Ninomiya, Masayuki Yoshikawa, Osamu Muraoka. Total Synthesis of 4,5-Didehydroguadiscine: A Potent Melanogenesis Inhibitor from the Brazilian Medicinal Herb, Hornschuchia obliqua. Journal of natural products. 2015 Jul; 78(7):1536-42. doi: 10.1021/np500995z. [PMID: 26135746]
  • Souichi Nakashima, Yoshimi Oda, Seikou Nakamura, Jiang Liu, Koko Onishi, Miki Kawabata, Hisako Miki, Yugo Himuro, Masayuki Yoshikawa, Hisashi Matsuda. Inhibitors of melanogenesis in B16 melanoma 4A5 cells from flower buds of Lawsonia inermis (Henna). Bioorganic & medicinal chemistry letters. 2015 Jul; 25(13):2702-6. doi: 10.1016/j.bmcl.2015.04.052. [PMID: 25987378]
  • Alessia Panusa, Rita Petrucci, Giancarlo Marrosu, Giuseppina Multari, Francesca Romana Gallo. UHPLC-PDA-ESI-TOF/MS metabolic profiling of Arctostaphylos pungens and Arctostaphylos uva-ursi. A comparative study of phenolic compounds from leaf methanolic extracts. Phytochemistry. 2015 Jul; 115(?):79-88. doi: 10.1016/j.phytochem.2015.01.002. [PMID: 25702282]
  • Elżbieta Kuźniak, Marzena Wielanek, Grażyna Chwatko, Rafał Głowacki, Marta Libik-Konieczny, Milena Piątek, Ewa Gajewska, Maria Skłodowska. Salicylic acid and cysteine contribute to arbutin-induced alleviation of angular leaf spot disease development in cucumber. Journal of plant physiology. 2015 Jun; 181(?):9-13. doi: 10.1016/j.jplph.2015.03.017. [PMID: 25955697]
  • Yan Wu, Zheng-Rong Wu, Peng Chen, Yang-Li, Wan-Rong Deng, You-Quan Wang, Hong-Yu Li. Effect of the tyrosinase inhibitor (S)-N-trans-feruloyloctopamine from garlic skin on tyrosinase gene expression and melanine accumulation in melanoma cells. Bioorganic & medicinal chemistry letters. 2015 Apr; 25(7):1476-8. doi: 10.1016/j.bmcl.2015.02.028. [PMID: 25726329]
  • María Del Carmen Avelino-Flores, María del Carmen Cruz-López, Fabiola E Jiménez-Montejo, Julio Reyes-Leyva. Cytotoxic activity of the methanolic extract of Turnera diffusa Willd on breast cancer cells. Journal of medicinal food. 2015 Mar; 18(3):299-305. doi: 10.1089/jmf.2013.0055. [PMID: 25299247]
  • Xu-Lu Luo, Na Li, Min Xu, Hong-Tao Zhu, Peng He, Yong Ding, Ping Zhao, Ying-Jun Zhang. HPLC simultaneous determination of arbutin, chlorogenic acid and 6'-O-caffeoylarbutin in different parts of Vaccinium dunalianum Wight. Natural product research. 2015; 29(20):1963-5. doi: 10.1080/14786419.2015.1013472. [PMID: 25716538]
  • Sroka Zbigniew, Żbikowska Beata, Janicki Kamil, Franiczek Roman, Krzyżanowska Barbara, Dryś Andrzej. Antimicrobial and antiradical activity of extracts obtained from leaves of three species of the genus pyrus. Microbial drug resistance (Larchmont, N.Y.). 2014 Aug; 20(4):337-43. doi: 10.1089/mdr.2013.0155. [PMID: 24621262]
  • Gian Maria Busetto, Riccardo Giovannone, Matteo Ferro, Stefano Tricarico, Francesco Del Giudice, Deliu Victor Matei, Ottavio De Cobelli, Vincenzo Gentile, Ettore De Berardinis. Chronic bacterial prostatitis: efficacy of short-lasting antibiotic therapy with prulifloxacin (Unidrox®) in association with saw palmetto extract, lactobacillus sporogens and arbutin (Lactorepens®). BMC urology. 2014 Jul; 14(?):53. doi: 10.1186/1471-2490-14-53. [PMID: 25038794]
  • Tanja R Scheublin, Simon Deusch, Silvia K Moreno-Forero, Jochen A Müller, Jan Roelof van der Meer, Johan H J Leveau. Transcriptional profiling of Gram-positive Arthrobacter in the phyllosphere: induction of pollutant degradation genes by natural plant phenolic compounds. Environmental microbiology. 2014 Jul; 16(7):2212-25. doi: 10.1111/1462-2920.12375. [PMID: 24373130]
  • Yukiko Yamashita-Higuchi, Sachiko Sugimoto, Katsuyoshi Matsunami, Hideaki Otsuka, Takahito Nakai. Grevillosides J-Q, arbutin derivatives from the leaves of Grevillea robusta and their melanogenesis inhibitory activity. Chemical & pharmaceutical bulletin. 2014; 62(4):364-72. doi: 10.1248/cpb.c13-00962. [PMID: 24695346]
  • Min Xu, Qiao-Cong Lao, Ping Zhao, Xiao-Yu Zhu, Hong-Tao Zhu, Xu-Lu Luo, Chong-Ren Yang, Jian-Hui He, Chun-Qi Li, Ying-Jun Zhang. 6'-O-Caffeoylarbutin inhibits melanogenesis in zebrafish. Natural product research. 2014; 28(12):932-4. doi: 10.1080/14786419.2014.883395. [PMID: 24498931]
  • Chizuru Sasaki, Masaki Ichitani, Ko-Ki Kunimoto, Chikako Asada, Yoshitoshi Nakamura. Extraction of arbutin and its comparative content in branches, leaves, stems, and fruits of Japanese pear Pyrus pyrifolia cv. Kousui. Bioscience, biotechnology, and biochemistry. 2014; 78(5):874-7. doi: 10.1080/09168451.2014.893185. [PMID: 25035992]